The stereoselective preparation of 1-hydroxycyclopenta-precursors are easily synthesized by two consecutive enolate alkylations. Excellent stereochemical control for the necarboxylic acid derivatives is reported. The key reaction is either a radical cyclization or a radical annulation mediated quate
β¦ LIBER β¦
ChemInform Abstract: Preparation of 1-Hydroxycyclopentanecarboxylic Acid Derivatives from a Chiral Equivalent of Glycolic Acid.
β Scribed by Sokol Abazi; Liliana Parra Rapado; Kurt Schenk; Philippe Renaud
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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